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3344 Health-Related Quality of Life in Polish Patients with Multiple Myeloma Treated in the Phase 3 ATLAS Trial of Post-Transplant Maintenance with Carfilzomib, Lenalidomide, Dexamethasone or Lenalidomide Alone

Program: Oral and Poster Abstracts
Session: 652. Multiple Myeloma: Clinical and Epidemiological: Poster II
Hematology Disease Topics & Pathways:
Research, Clinical Research, patient-reported outcomes
Sunday, December 10, 2023, 6:00 PM-8:00 PM

Tadeusz Kubicki1,2*, Ben A Derman, MD3, Krzysztof Jamroziak4*, Pawel Robak5*, Jaroslaw Czyz6*, Agata Tyczynska7*, Agnieszka Druzd-Sitek8*, Krzysztof Giannopoulos9*, Tomasz Wrobel, MD, PhD10*, Adam Nowicki2*, Tomasz Szczepaniak2*, Anna Lojko-Dankowska2*, Magdalena Matuszak2*, Lidia Gil2, Bartosz Michal Pula4*, Lukasz Szukalski6*, Agnieszka Konska4*, Jan M. Zaucha7*, Jan Walewski8, Damian Mikulski5*, Olga Czabak11*, Tadeusz Robak5*, Dorota Kruk-Kwapisz12*, Andrzej J Jakubowiak, MD, PhD1 and Dominik Dytfeld2*

1University of Chicago, Chicago, IL
2Poznan University of Medical Sciences, Poznan, Poland
3University of Chicago, CHICAGO, IL
4Institute of Hematology and Blood Transfusion, Warsaw, Poland
5Medical University of Lodz, Lodz, Poland
6Nicolaus Copernicus University in Torun Ludwik Rydygier, Collegium Medicum in Bydgoszcz, Bydgoszcz, Poland
7Medical University of Gdansk, Gdansk, Poland
8Maria Sklodowska-Curie National Research Institute of Oncology, Warszawa, Poland
9Department of Experimental Hematooncology, Medical University of Lublin, Lublin, Poland
10Wroclaw Medical University, Wroclaw, Poland
11Medical University of Lublin, Lublin, Poland
12Clinscience, Warsaw, Poland

Introduction

Results of the unplanned interim analysis of the ATLAS trial (Dytfeld, Lancet Oncology 2023) suggest a progression-free survival benefit of carfilzomib, lenalidomide, and dexamethasone (KRd) post-transplant maintenance over single-agent lenalidomide (R). Use of triplet combination, with frequent hospital visits and repeated intravenous infusions raises questions about its long-term tolerability and the impact on health-related quality of life (HRQoL) compared with relatively convenient and well-tolerated single-agent oral lenalidomide. Here, we present a descriptive, longitudinal assessment of HRQoL in Polish patients with multiple myeloma treated in the ATLAS trial.

Methods

ATLAS is an ongoing phase 3 trial that randomized 180 patients with newly-diagnosed multiple myeloma after ASCT to receive maintenance therapy with KRd or R. In the KRd arm, patients with standard-risk cytogenetics who achieved MRD-negativity after cycle 6 de-escalated therapy to receive R alone after cycle 8. HRQoL assessment was not required by the study protocol, however, the FACT/GOG-Ntx questionnaires were collected according to local protocols for post-transplant data collection at 7 Polish sites at screening (approximately 3 months post-transplant) and after cycles (C) 6, 12, 18, 24, 30, and 36. Therefore, the modified intention-to-treat (mITT) population in this analysis consisted of 134 patients enrolled in these sites. The domains evaluated by the FACT/GOG-Ntx questionnaire include physical well-being (PWB), social well-being (SWB), emotional well-being (EWB), functional well-being (FWB), and neurotoxicity (Ntx). The outcomes are summarized in FACT/GOG-Ntx Trial Outcome Index (TOI, combining PWB, FWB, and Ntx), FACT-G Total Score (PWB, SWB, EWB, and FWB), and FACT/GOG-Ntx Total Score (all five domains). Based on previous reports, the minimally important difference (MID) was defined as a change of at least 10% of the instrument range (Tremblay, BMC Cancer 2021). Student’s t-test was used for comparisons between normally distributed variables and Wilcoxon rank-sum test for not normally distributed. Rates of patients experiencing MID were compared using chi-square test.

Results

HRQoL questionnaires were available for 123 out of 134 patients (92%). The numbers of completed questionnaires at screening, C6, C12, C18, C24, C30, C36 were 115 (86% of randomized patients / 86% of expected patients), 111 (83%/86%), 102 (76%/85%), 93 (69%/85%), 82 (61%/86%), 74 (55%/87%), and 56 (42%/80%), respectively. Throughout the analyzed timepoints, the mean PWB, SWB, EWB, FWB, NTx scores (Figure 1), FACT/GOG-NTx TOI, FACT-G Total Score, and FACT/GOG-Ntx Total Score (Figure 2) did not differ between the two study arms. A similar pattern was observed in the changes in individual patient scores compared to baseline. During the treatment course, the rates of patients experiencing a decrease in HRQoL scores, reaching the MID threshold in at least one evaluation, were consistent in both groups – 19 out of 59 (32%) patients treated with KRd and 20 out of 52 (38%) patients in the R arm (p=0.49) in the FACT/GOG-NTx TOI, 23/59 (39%) in the KRd arm and 21/52 (40%) in the R arm in the FACT-G Total Score (p=0.88), and 24/59 (41%) in the KRd arm and 19/52 (37%) in the R arm in the FACT/GOG-Ntx Total Score (p=0.65). Similarly, there were no differences in the respective results in terms of patients experiencing an increase in HRQoL scores, reaching the MID threshold in at least one evaluation – 8 out of 59 (14%) patients treated with KRd and 11 out of 52 (21%) patients in the R arm (p=0.28) in the FACT/GOG-NTx TOI, 10/59 (17%) in the KRd arm and 13/52 (25%) in the R arm in the FACT-G Total Score (p=0.29), and 8/59 (14%) in the KRd arm and 6/52 (12%) in the R arm in the FACT/GOG-Ntx Total Score (p=0.75).

Conclusions

The results of this analysis do not imply a negative impact of post-transplant maintenance with carfilzomib, lenalidomide, and dexamethasone compared to single-agent lenalidomide on the HRQoL.

Disclosures: Derman: Janssen: Consultancy, Honoraria; COTA Healthcare: Consultancy. Wrobel: Roche, Takdea, Novartis, BMS, Celgene, Janssen-Cilag, Beigene, Gilead, Sanofi: Honoraria; Roche: Research Funding; Roche, Novartis, Takeda, Celgene, BMS, Janssen-Cilag, Beigene, Sanofi: Speakers Bureau; Gilead, Roche, Takeda: Other: Travel, Accomodations, Expenses; Roche, Novartis, Takeda,Celgene, BMS, Janssen-Cilag, Beigene, Pfizer, Gilead, Sanofi, GSK: Consultancy. Gil: Celgene/BMS: Honoraria; Janssen: Honoraria; Gilead: Honoraria, Membership on an entity's Board of Directors or advisory committees; Abbvie: Honoraria; Astellas: Honoraria; Novartis: Honoraria; Pfizer: Honoraria. Zaucha: Medical University of Gdańsk: Current Employment; BMS: Research Funding; Pierre Fabre, Takeda, BMS, Gilead, Novartis, Pfizer, Amgen, F. Hoffmann-La Roche Ltd, Astra Zeneca, Abbvie: Honoraria; MSD: Research Funding. Walewski: Amgen: Honoraria; Gilead: Consultancy, Honoraria; Novartis: Consultancy, Honoraria; Roche: Consultancy, Honoraria, Research Funding; Takeda: Consultancy, Honoraria; GSK/Novartis: Research Funding; Servier: Honoraria; Abbvie: Consultancy, Honoraria. Robak: Janssen: Consultancy, Honoraria, Research Funding; Abbvie: Honoraria; OctoPharma: Honoraria, Research Funding; BeiGene: Honoraria, Research Funding; GSK: Honoraria, Research Funding; AstraZeneca: Honoraria, Research Funding; Regeneron: Honoraria, Research Funding. Kruk-Kwapisz: Clinscience: Current Employment. Jakubowiak: Abbvie: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; GSK: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Sanofi-Aventi: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Amgen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; BMS: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees. Dytfeld: BMS: Honoraria, Membership on an entity's Board of Directors or advisory committees; Amgen: Honoraria, Membership on an entity's Board of Directors or advisory committees.

OffLabel Disclosure: Carfilzomib, Lenalidomide, dexamethasone combination as maintenance therapy post autologous stem cell transplantation in multiple myeloma.

*signifies non-member of ASH